Employer King's College Hospital NHS Foundation Trust Employer type NHS Site Kings College Hospital Foundation NHS Trust Town London Salary £37,259 - £45,356 per annum inc HCA's Salary period Yearly Closing 08/12/2025 08:00 Interview date 18/12/2025
Job overview
The post-holder will report to the Lead Paediatric Research Nurse who is responsible for managing the requirements and demands for research delivery support across the research programmes and themes at the Trust; the candidate will be based at the Paediatric Research Office at King's College Hospital and will work in close liaison, building excellent relationships with the study principal investigators at King's College Hospital NHS Foundation Trust and at the Princess Royal University Hospital (PRUH) site in Orpington. The paediatric research portfolio includes commercial and non-commercial studies across a variety of different specialities including haematology, liver, gastroenterology, respiratory, paediatric intensive care, neonatal and neurosurgical; the post holder will be given the opportunity to gain research experience across these fields with training and support from the team.
The post-holder will be required to monitor and update recruitment for their studies on the EDGE portal; they will ensure that any research undertaken at this recruiting site safeguards the well-being of patients and is conducted according to Good Clinical Practice (GCP) and the Medicines for Human Use (Clinical Trial) Regulations **** and Amended Regulations ****.
The post holder will undertake all relevant responsibilities as study co-ordinator and will ensure that they maintain high quality standards throughout the study thus ensuring excellent data integrity.
Main duties of the job
Manage own study portfolio within the designated areas of responsibility.
Maintain effective communication with patients, parents, carers and professionals to ensure service delivery.
Adhere to King's Policy and procedures.
Be responsible for the whole patient recruitment process from selection to screening and from randomisation to the scheduling of study visits.
Evaluate patient eligibility for the trial during pre-screening. Liaising with the investigator. Co-ordinating pre-study tests, obtaining results and arranging appropriate appointments according to the Schedule of Events in the study protocols.
Ensure patients are fully informed prior to entry into the clinical research programme. To provide ongoing advice and information to patients with regards to their participation in clinical research in order to facilitate effective informed consent.
Offer support to patients and families, explaining practical aspects of the trial, assisting and supporting local nursing teams when necessary.
Follow the principles of Good Clinical Practice (GCP) and ensure that the trial is conducted according to the Medicines for Human Use (Clinical Trial) Regulations **** and Amended Regulations **** where appropriate.
Maintain clear and accurate data when transcribing data onto electronic or paper case report forms.
Working for our organisation
King's College Hospital NHS Foundation Trust is one of the UK's largest and busiest teaching Trusts with a turnover of £1 billion, 1.5 million patient contacts a year and around 14,000 staff based across 5 main sites in South East London. The Trust provides a full range of local hospital services across its different sites, and specialist services from King's College Hospital (KCH) sites at Denmark Hill in Camberwell and at the Princess Royal University Hospital (PRUH) site in Bromley.
King's is committed to delivering Sustainable Healthcare for All via our Green Plan. In line with national Greener NHS ambitions, we have set net zero carbon targets of **** for our NHS Carbon Footprint and **** for our NHS Carbon Footprint Plus. Everyone's contribution is required in order to meet the goals set out in our Green Plan and we encourage all staff to work responsibly, minimising their contributions to the Trust's carbon emissions, waste and pollution wherever possible.
The trust-wide strategy Strong Roots, Global Reach is our Vision to be BOLD, Brilliant people, Outstanding care, Leaders in Research, Innovation and Education, Diversity, Equality and Inclusion at the heart of everything we do. By being person-centred, digitally-enabled, and focused on sustainability, we can take Team King's to another level.
Detailed job description and main responsibilities
The successful candidate will have the opportunity to learn about research governance, ethics, study management and study delivery with an introduction to research finance.
All relevant and mandatory research training will be provided.
The successful candidate will be part of a team that manages a portfolio of interesting clinical trials in various disorders in Paediatric research.
The successful candidate will carry out patient recruitment, study assessments, blood collection and processing, data entry and data management alongside administrative tasks as needed for the clinical trials activities within RDU 9.
The successful candidate will gain experience in running commercial and non-commercial clinical trials by carrying out research activities, aimed at improving the care and treatment of the paediatric patients.
The successful candidate will develop a close working relationship with the inpatient and outpatient support services and be invited to the clinical trial team meetings.
The successful candidate will work towards being proficient in managing his/her own research workload effectively and completing trial documentation accurately and in a timely manner.
If you would like to find out more and wish to arrange an informal visit then please contact Katie Tupper ************* or via email:
Person specification
Education and Qualifications
NMC registered Children's Nurse- Children's nursing qualification
Research Training
Good Clinical Practice Certification
Human Tissue Authority and Consent Training
Experience
Experience working in the paediatric clinical setting as a registered children's nurse
Research experience
Experience in liaising with study monitors and sponsors
Experience in maintaining study data bases
Experience in reporting SAEs within the 24-hour deadline
Knowledge
Knowledge of NHS/clinical setting
Awareness of the need for discretion and confidentiality
A good understanding of research governance and ethics
Research Invoicing
Skills
Good communication and personal skills
Computer literacy and competence in standard PC packages.
Venepuncture and cannulation
Abilities
Ability to work under pressure
Ability to work independently and as part of a team
Ability to impart study information to patients, relatives and carers, with different levels of understanding
Ability to enter data onto sponsors' EDC systems accurately and in a timely manner
Ability to interact sensitively and professionally with clinical staff and patients
Adaptable and flexible
Punctual and dependable
Willing to learn new skills
Maintains a professional image
Motivated and enthusiastic
Employer certification / accreditation badges
You must have appropriate UK professional registration.
This post is subject to the Rehabilitation of Offenders Act **** (Exceptions) Order **** (Amendment) (England and Wales) Order **** and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service.
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